Desiree Nock-Chester

CRS:

JHU

Role:

Research Staff

Position:

Research Assistant

Email:

dnock1@jhmi.edu

Desiree Nock-Chester responsible for QA/QC. Her duties include QA/QC of charts and crf binders, visit prep, creating laboratory requisitions, resolving queries and delinquencies, transcription, data entry, and maintaining error reports.

She has been a part of the data staff of the ACTG  at Johns Hopkins University for more than 10 years. She began as the transcriptionist for the unit and held that position for nearly 3 years. Prior to joining the clinical trials unit, Ms. Nock-Chester worked in the Wilmer at  Johns Hopkins for 9 years as a Sr. Patient Services Coordinator. Her  duties included registering patients for appointments, surgeries, post-op visits, verifying insurance information, obtaining referrals, and balancing out the daily intake of co-payments.

Categories

Leadership Committees
CRS
Roles

Clinical Trials

A5302:  BioBank for Surrogate Marker Research for TB...

Primary Objective To obtain sputum, serum, urine, and peripheral blood mononuclear cells (PBMCs) for central TB biorepository...

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A5128: Consent for Use of Stored Patient Specimens for...

The purpose of this study is to obtain informed consent to use stored human biological materials (HBM) (e.g., blood and other...

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P1077BF: Breastfeeding Version of the PROMISE Study...

1077BF is a randomized strategy trial, which is part of the PROMISE studies (1077BF, 1077FF, P1084s, and 1077HS). The Promoting...

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A5384: A Phase II, Randomized, Open-Label Trial of a...

Study Description A5384 is a trial for people who have or might have tuberculous meningitis (TBM). TBM is an infectious disease...

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IMPAACT 2034 - Phase I Study of the Pharmacokinetics,...

This is a Phase I, multi-site, open-label, non-comparative study of the PK, safety, tolerability, and acceptability of a...

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